Company Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions..., Compliance, Computer, Engineering, Project Management, Validation, and other services. Job Description We are seeking...
Validation Engineer position reports into the Sr. Manager of Validation. This position requires the application of diverse... facility. Responsibilities: The Senior Validation Engineering will support the development and implementation of automated...
Job Title: Senior Packaging Validation Engineer, Biotech GMP Final Drug Product (JP14454) Location: New Albany, Oh...! We are recruiting a Senior Validation Engineer for a consulting engagement with our direct client, a leading global biotechnology...
Payrate: $53.00 - $55.00/hr. Summary: The Senior Validation Engineer position reports into the Sr. Manager... of Validation. This position requires the application of diverse and advanced engineering and scientific principles in support...
. What you will do Let’s do this. Let’s change the world. In this role the Senior Engineer position reports to the Sr, Manager of Validation... Development team where the candidate must manage and/or apply extensive technical expertise in the qualification and validation...
Validations Specialist is responsible for developing, executing, and maintaining validation protocols and reports related... with applicable regulatory requirements, internal quality standards, and industry best practices for process validation, cleaning...
: Work alongside various departments to ensure safety and efficiency in all operations. Design Validation: Assess designs...
Validation: Assess designs for strength and conformity to accepted standards and integrate vendor specifications into your work...
, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements... with validation processes for Packaging areas Familiarity with serialization process and networking Familiarity with documentation...
to support material inventory system (SAP transactions) and electronic batch records. Oversight of equipment/process validation...
, quality assurance and/or validation departments in developing requirements and recommendations for system modifications... with validation processes for Packaging areas Familiarity with serialization process and networking Familiarity with documentation...
, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments... Familiarity with validation processes for Packaging areas Familiarity with serialization process and networking Familiarity...
, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments... of pharmaceutical/biotech processes Familiarity with validation processes for Packaging areas Familiarity with serialization process...
/environmental, technical cleaning, validation, electrical, and process automation issues. Assist during regulatory agency... inspections. Provide technical support in response to the FDA and other regulatory agencies. Support cGMP validation of equipment...
support in response to the FDA and other regulatory agencies. Support cGMP validation of equipment and processes. Complete...
on engineering, regulatory, compliance, calibration, quality, microbial/environmental, technical cleaning, validation, electrical... and other regulatory agencies. Support cGMP validation of equipment and processes. Complete advanced maintenance activities or operate...
assembly. Lead commissioning, qualification, and validation (CQV) of GMP equipment. Own and maintain the site master... validation plan. Operational Excellence: Analyze, design, and implement manufacturing/business process improvements...
, and validation (CQV) of GMP equipment. Own and maintain the site master validation plan. Operational Excellence: Analyze... & Packaging Equipment: Strong knowledge of automated and semi-automated device assembly, validation, and troubleshooting...
device assembly. Lead commissioning, qualification, and validation (CQV) of GMP equipment. Own and maintain the site master... validation plan. Operational Excellence: Analyze, design, and implement manufacturing/business process improvements. Drive...
Strong knowledge of automated and semi-automated device assembly, validation, and troubleshooting Experience in GMP-Regulated..., qualification, and validation activities for GMP equipment, including ownership of the sites master validation plan. Support...